Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
  • C07B35/00—Reactions without formation or introduction of functional groups containing hetero atoms, involving a change in the type of bonding between two carbon atoms already directly linked
  • C07B35/06—Decomposition, e.g. elimination of halogens, water or hydrogen halides
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
  • C07C1/26—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only halogen atoms as hetero-atoms
  • C07C1/30—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only halogen atoms as hetero-atoms by splitting-off the elements of hydrogen halide from a single molecule
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C67/00—Preparation of carboxylic acid esters
  • C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
  • C07C67/317—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
  • C07C2531/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
  • C07C2531/24—Phosphines
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C2601/00—Systems containing only non-condensed rings
  • C07C2601/02—Systems containing only non-condensed rings with a three-membered ring

Definitions

• the present invention relates to a hydrodehalogenation method in which a halogen atom on a carbon atom of an organic compound is removed by substituting the halogen atom with a hydrogen atom, and to a method for producing a dehalogenated compound.
• Organic halogen compounds having a halogen atom such as chlorine are generally harmful to living organisms as exemplified by PCBs and dioxins. These compounds are stable and hardly degradable in the natural environment, therefore, if they are once released to the environment, these compounds are accumulated to contaminate the environment. Even such harmful organic halogen compounds, they can be rendered harmless or low-toxic through removal of halogen in the compounds (i.e., dehalogenation).
• dehalogenation methods include chemical extraction and decomposition, decomposition with metallic sodium, hydroxylation with supercritical water, and also, incineration is carried out for rendering these compounds harmless or non-toxic.
• dehalogenation techniques require considerably severe reaction conditions, cost for plants and apparatus is disadvantageously high.
• Patent Document 1 JP-A-2005-82539
• Non-Patent Document 1 R. Boukherroub et al., Organometallics, 15, 1508, 1996
• Non-Patent Document 2 Miguel A. Esteruelas et al., Organometallics, 18, 1110, 1999
• Non-Patent Document 3 H. Guo et al., Chemistry Letter, 33, 10, 1356, 2004
• An object of the present invention is to provide a hydrodehalogenation method which employs a reagent that allows scaling-up of hydrodehalogenation to an industrial level and which realizes simple and effective removal of a halogen atom from an organic halogen compound by substituting the halogen atom with a hydrogen atom.
• the present inventors have carried out extensive studies on hydrodehalogenation reaction of organic halogen compounds, and have found that, through treating an organic halogen compound in the presence of a catalytic amount of a Group VIII metal complex and a hydrogen source, a dehalogenated compound can be produced at high yield, and that a reducing reagent, which is inexpensive and allows easy handling, can be employed as a hydrogen source.
• the present invention has been accomplished on the basis of these findings.
• the present invention is directed to a hydrodehalogenation method including treating an organic compound having a halogen atom on a carbon atom thereof in a solvent with a compound represented by formula (2-1): M 2 BH p R 1 q (2-1) or formula (2-2): M 3 (BH p R 1 q ) 2 (2-2) (wherein M 2 represents an alkali metal atom; M 3 represents an alkaline earth metal atom or a zinc atom; R 1 represents a hydrogen atom, a cyano group, a C2-C13 acyloxy group, or a C1-C6 alkoxy group; p is an integer of 1 to 4; q is an integer of 0 to 3; and the sum of p and q is 4) in the presence of a Group VIII metal complex represented by formula (1): M 1 X m L n (1) (wherein M 1 represents a Group VIII metal; X represents a halogen atom; L represents a neutral
• the present invention is also directed to a method for producing a dehalogenated compound, characterized by comprising treating an organic compound having a halogen atom on a carbon atom thereof in a solvent with a compound represented by formula (2-1): M 2 BH p R 1 q (2-1) or formula (2-2): M 3 (BH p R 1 q ) 2 (2-2) (wherein M 2 represents an alkali metal atom; M 3 represents an alkaline earth metal atom or a zinc atom; R 1 represents a hydrogen atom, a cyano group, a C2-C13 acyloxy group, or a C1-C6 alkoxy group; p is an integer of 1 to 4; q is an integer of 0 to 3; and the sum of p and q is 4) in the presence of a Group VIII metal complex represented by formula (1): M 1 X m L n (1) (wherein M 1 represents a Group VIII metal; X represents a halogen
• the hydrodehalogenation method according to the present invention employing a metal borohydride compound as a hydrogen source, has been realized as industrially applicable, which is difficult to be accomplished through a previous method from the viewpoints of cost and operability. Furthermore, the present invention is remarkably advantageous, since hydrodehalogenation of an organic halogen compound such as an aromatic halogen compound (e.g., an endocrine-disrupting chemical) which is harmful and hardly degradable can be completed under relatively mild conditions. Best Modes for Carrying Out the Invention
• the Group VIII metal complex employed in the present invention is a compound represented by formula (1):
• M 1 represents a Group VIII metal such as rhodium, palladium, ruthenium, platinum, cobalt, or nickel. Among these, rhodium and palladium are preferred, with rhodium being particularly preferred.
• halogen atom represented by X examples include fluorine, chlorine, bromine, and iodine.
• L represents a neutral ligand.
• the species of the neutral ligand include phosphine, trialkylamine, nitrile, isonitrile, diene, arene, carbonyl, carbene, alkene, alkyne, cyclobutadiene, cycloheptatriene ether, olefin, and thioether.
• phosphine PR 2 R 3 R 4
• PR 2 R 3 R 4 are preferably employed.
• R 2 , R 3 , and R 4 which may be the same or different, each represents an aliphatic (hydrocarbon) group or aromatic (hydrocarbon) group.
• aromatic group examples include C6-C14 aromatic hydrocarbon groups such as phenyl and naphthyl, and C6-C14 aromatic hydrocarbonoxy groups such as phenoxy. These groups may be substituted by one or more ordinary employed functional groups.
• the aliphatic group examples include C1-C30 alkyl groups and C1-C30 alkoxy groups, which may be linear, branched, or cyclic.
• Specific examples include methyl, ethyl, propyl, isopropyl, tert-butyl, pentyl, hexyl, methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, sec-butoxy, tert-butoxy, and cyclopentyloxy.
• phosphine ligand examples include tertiary phosphines such as trimethylphosphine, triethylphosphine, tripropylphosphine, tributylphosphine, tricyclohexylphosphine, triphenylphosphine, dimethylphenylphosphine, diphenylmethylphosphine, 2-di-tert-butylphosphino-1,1'-binaphthyl, 2-(di-tert-butylphosphino)biphenyl, 2-di-tert-butylphosphino-2'-(N,N-dimethylamino)biphenyl, 2-di-tert-butylphosphino-2'-methylbiphenyl, 2-(dicyclohexylphosphino)biphenyl, 2-dicyclohexylphosphino-2',6'-dimethoxy-1,1
• Compound (1) examples include RhCl(PPh 3 ) 3 (Wilkinson's complex), RuCl 2 (PPh 3 ) 2 , NiCl 2 (PPh 3 ) 2 , PdCl 2 (PPh 3 ) 2 , CoCl 2 (PPh 3 ) 2 , and CoCl(PPh 3 ) 3 .
• RhCl(PPh 3 ) 3 (Wilkinson's complex) is particularly preferably employed.
• the Group VIII metal complex (1) is preferably used in an amount of 0.03 to 1 mole equivalent, with respect to the organic halogen compound, more preferably 0.05 to 0.5 mole equivalents.
• the Group VIII metal complex (1) may be a commercial product or may be prepared from a corresponding Group VIII metal salt and a neutral ligand.
• the hydrogen source (reducing agent) employed in the method of the present invention is a compound represented by M 2 BH p R 1 q (2-1) or M 3 (BH p R 1 q ) 2 (2-2) (hereinafter referred to as Compound (2-1) or Compound (2-2)).
• M 2 represents an alkali metal atom such as lithium, sodium, or potassium. Of these, lithium and sodium are more preferred, with sodium being particularly preferred.
• M 3 represents an alkaline earth metal atom such as magnesium, calcium, or strontium, or a zinc atom. M 3 is preferably calcium or zinc.
• R 1 represents a hydrogen atom, a cyano group, a C1-C6 alkoxy group, or a C2-C13 acyloxy group.
• the C1-C6 alkoxy group may be a linear or branched C1-C6 alkoxy group or a C3-C6 cycloalkyloxy group, and examples include methoxy, ethoxy, and cyclopentyloxy.
• the C2-C13 acyloxy group may be an alkylcarbonyloxy group, an arylcarbonyloxy group, or an aralkylcarbonyloxy group.
• a C2-C13 acyloxy groups a C2-C7 acyloxy group is preferred.
• C2-C7 acyloxy group examples include an acetyloxy group, a trifluoroacetyloxy group, a benzoyloxy group, and a benzylcarbonyloxy group; and also include an N-isobutyloxycarbonylprolyloxy group and an N-benzyloxycarbonylprolyloxy group.
• p is an integer of 1 to 4
• q is an integer of 0 to 3
• the sum of p and q is 4.
• Examples of Compound (2-1) or Compound (2-2) include sodium borohydride, lithium borohydride, zinc borohydride, calcium borohydride, sodium cyanoborohydride, and sodium alkoxyborohydride. Of these, sodium borohydride is particularly preferably employed.
• Compound (2-1) or Compound (2-2) is preferably employed in an amount of 1.0 to 10.0 mole equivalents with respect to the organic halogen compound, more preferably 1.1 to 3.0 mole equivalents.
• reaction solvent employed in the method of the present invention, and any solvent may be used so long as it does not inhibit reactions.
• solvents examples of hydrocarbons, which may be aliphatic or aromatic, include n-hexane, n-pentane, benzene, toluene, and xylene.
• examples of alcohols include methanol, ethanol, propanol, isopropanol (IPA), n-butanol, and t-butanol.
• ethers include diethyl ether, diisopropyl ether (IPE), methyl t-butyl ether (MTBE), tetrahydrofuran (THF), cyclopentyl methyl ether, dimethoxyethane, and 1,4-dioxane.
• amides include dimethylformamide (DMF), dimethylacetamide (DMAc), and N-methyl-2-pyrrolidone (NMP).
• cyclic ureas include 1,3-dimethyl-2-imidazolidinone (DMI) and 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone (DMPU).
• halogenohydrocarbons examples include chloroform, methylene chloride, and 1,2-dichloroethane (EDC).
• Other solvents such as water, dimethylsulfoxide (DMSO), sulfolane, acetonitrile, acetic acid esters, and acetone may also be used. These solvents may be used singly or in combination of a plurality of species.
• amides such as dimethylformamide (DMF), N-methyl-2-pyrrolidone (NMP), and dimethylacetamide (DMAc); alcohols such as methanol, ethanol, and isopropanol (IPA); dimethylsulfoxide; ethyl acetate; and tetrahydrofuran (THF) are preferred, with amides such as N-methyl-2-pyrrolidone (NMP) and dimethylacetamide (DMAc) and alcohols such as isopropanol being more preferred, with amides such as N-methyl-2-pyrrolidone (NMP) and dimethylacetamide (DMAc) being particularly preferred.
• DMF dimethylformamide
• NMP N-methyl-2-pyrrolidone
• DMAc dimethylacetamide
• the solvent is used in a total amount of 1 to 20 (v/w) with respect to the Group VIII metal complex (1), more preferably 3 to 10 (v/w).
• the reaction temperature may be 0°C to the boiling point of the solvent employed, and is particularly preferably 50 to 80°C.
• an organic halogen compound is hydrodehalogenated. Specifically, a halogen atom of an organic halogen compound is substituted with a hydrogen atom, thereby removing the halogen atom.
• the halogen atom to be removed is a halogen atom on a carbon atom, and is substituted with a carbon atom constituting an aromatic compound or an aliphatic compound. Therefore, the compounds to which the method of the present invention can be applied are aromatic halogen compounds and aliphatic halogen compounds.
• the "aromatic compound,” may be an aromatic hydrocarbon compound or an aromatic heterocyclic compound, and may be monocyclic or polycyclic.
• Examples of the "monocyclic aromatic compound” include benzene and 5- or 6-membered aromatic heterocyclic compounds.
• Examples of “5- or 6-membered heterocyclic compounds” include furan, thiophene, pyrrole, pyran, thiopyran, pyridine, thiazole, imidazole, pyrimidine, and 1,3,5-triazine.
• polycyclic aromatic compound examples include polycyclic aromatic hydrocarbon compounds and polycyclic heteroaromatic compounds.
• polycyclic aromatic hydrocarbon compounds include biphenyl, triphenyl, naphthalene, indene, anthracene, and phenanthrene
• polycyclic heteroaromatic compounds examples include indole, quinoline, and purine.
• the aromatic halogen compound has a basic structure of the aforementioned "aromatic compound" to which one or more halogen atoms have been introduced at substitutable positions.
• halogen atoms Preferably, 1 to 4 halogen atoms are introduced.
• the halogen atom include fluorine, chlorine, bromine, and iodine. Of these, fluorine and chlorine are preferred.
• fluorine, chlorine, bromine, and iodine may be introduced in any combination.
• One or more conventionally known functional groups may be introduced.
• examples of preferred aromatic halogen compounds include aromatic fluorine compounds and aromatic chlorine compounds, and specific examples include fluorobenzene, difluorobenzene, trifluorobenzene, tetrafluorobenzene, 1-fluoronaphthalene, 2-fluoronaphthalene, 2-fluoropyridine, 3-fluoropyridine, 6-fluoroquinoline, 7-fluoroquinoline, chlorobenzene, dichlorobenzene, trichlorobenzene, tetrachlorobenzene, 1-chloronaphthalene, 2-chloronaphthalene, 2-chloropyridine, 3-chloropyridine, 6-chloroquinoline, and 7-chloroquinoline.
• benzene can be recovered from any of the aforementioned halogenobenzene compounds. Similarly, from halogenonaphthalene compounds, halogenopyridine compounds, and halogenoquinoline compounds, naphthalene, pyridine, and quinoline can be recovered.
• the "aliphatic hydrocarbon compound,” which is a basic structure of the aliphatic halogenohydrocarbon compound, may be a chain hydrocarbon, an alicyclic hydrocarbon, etc.
• the chain hydrocarbon include a C 1 -C 20 alkane, a C 2 -C 20 alkene, and a C 2 -C 20 alkyne.
• the "C 1 -C 20 alkane” is preferably a C 1 -C 20 alkane, more preferably a C 1 -C 6 alkane. No particular limitation is imposed on the alkane, and examples include methane, ethane, propane, butane, pentane, and hexane.
• the "C 2 -C 20 alkene” is preferably a C 2 -C 20 alkene, with a C 2 -C 6 alkene being more preferred. No particular limitation is imposed on the alkene, and examples include ethene, propene, and butene.
• the "C 2 -C 20 alkyne” is preferably a C 2 -C 20 alkyne, with a C 2 -C 6 alkyne being particularly preferred. No particular limitation is imposed on the alkyne, and examples include acetylene, propyne, and butyne. These hydrocarbons may be linear or branched.
• the "alicyclic hydrocarbon” may be a C 3 -C 20 cycloalkane, a C 3 -C 20 cycloalkene, etc.
• the "C 3 -C 20 cycloalkane” is preferably a C 3 -C 10 cycloalkane. Examples of the cycloalkane include cyclopropane, cyclobutane, cyclopentane, and cyclohexane.
• the "C 3 -C 20 cycloalkene” is preferably a C 3 -C 10 cycloalkene.
• cycloalkene examples include cyclopropene, cyclobutene, cyclopentene, and cyclohexene.
• the unsaturated bond may be hydrogenated. If hydrodehalogenation is performed while the unsaturated bond is maintained, reaction conditions (e.g., low temperature) must be carefully selected.
• the aliphatic hydrocarbon halogen compound has a basic structure of the aforementioned "aliphatic hydrocarbon compound" to which one or more halogen atoms have been introduced at substitutable positions.
• halogen atoms Preferably, 1 to 4 halogen atoms are introduced.
• the halogen atom include fluorine, chlorine, bromine, and iodine. Of these, fluorine and chlorine are preferred.
• fluorine, chlorine, bromine, and iodine may be introduced in any combination.
• One or more conventionally known functional groups may be introduced.
• examples of preferred aliphatic halogenohydrocarbon compounds include aliphatic fluorohydrocarbon compounds, aliphatic chlorohydrocarbon compounds, and aliphatic chlorofluorohydrocarbon compounds.
• Specific examples preferred compounds include 1-chloro-2-fluorocyclopropanecarboxylic acid derivatives and 2-chloro-2-fluorocyclopropanecarboxylic acid derivatives. According to the method of the present invention, a cyclopropanecarboxylic acid compound can be recovered.
• the yield of benzene, as determined through high-performance liquid chromatography, was 94.9%, confirming that hydrodechlorination was successfully performed.
• the yield of benzene, as determined through high-performance liquid chromatography, was 88.8%, confirming that hydrodechlorination was successfully performed.
• the yield of benzene, as determined through high-performance liquid chromatography, was 94.8%, confirming that hydrodefluorination was successfully performed.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Applications Claiming Priority (2)

Publications (1)

Family

ID=37906301

Family Applications (1)

Country Status (4)

Cited By (1)

Families Citing this family (18)

Family Cites Families (8)

• 2006
  • 2006-10-05 US US12/089,211 patent/US20100130768A1/en not_active Abandoned
  • 2006-10-05 EP EP06811286A patent/EP1942087A1/de not_active Withdrawn
  • 2006-10-05 WO PCT/JP2006/319948 patent/WO2007040259A1/ja active Application Filing
  • 2006-10-05 JP JP2007538796A patent/JPWO2007040259A1/ja not_active Withdrawn

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events